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多发性硬化症患者接受干扰素-β和干扰素-β联合低剂量口服类固醇治疗后 Ki-67+自然杀伤细胞增加。

Increase of Ki-67+ natural killer cells in multiple sclerosis patients treated with interferon-β and interferon-β combined with low-dose oral steroids.

机构信息

Division of Clinical Neurology, University of Nottingham, Nottingham, United Kingdom.

出版信息

J Neuroimmunol. 2011 Jul;236(1-2):111-7. doi: 10.1016/j.jneuroim.2011.05.005. Epub 2011 Jun 8.

Abstract

Interferon-β (IFN-β) is known to expand regulatory CD56(bright) natural killer (NK) cells in multiple sclerosis (MS). In this cross-sectional study we show that MS patients treated with IFN-β alone or in combination with low-dose prednisolone displayed increased proportion of all NK cell subsets in the active phase of the cell cycle (Ki-67+). There was no difference in NK cell apoptosis markers. In vitro experiments showed that both IFN-β and IFN-β in combination with corticosteroids increased the proportion of Ki-67(+) NK cells. This study, although limited, shows that treatment with IFN-β affects NK cell cycle without altering NK cell apoptosis in MS patients.

摘要

干扰素-β(IFN-β)已知可扩增多发性硬化症(MS)患者中的调节性 CD56(bright)自然杀伤(NK)细胞。在这项横断面研究中,我们表明,接受 IFN-β 单独或联合低剂量泼尼松龙治疗的 MS 患者在细胞周期的活跃期(Ki-67+)显示出所有 NK 细胞亚群比例增加。NK 细胞凋亡标志物无差异。体外实验表明,IFN-β 和 IFN-β联合皮质类固醇均可增加 Ki-67(+)NK 细胞的比例。这项研究虽然有限,但表明 IFN-β 治疗可影响 MS 患者 NK 细胞周期,而不改变 NK 细胞凋亡。

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